Canonical Allele Identifier: CA238116422
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1026006063
MyVariant Identifiers: chr12:g.68550178C>T (hg19) chr12:g.68156398C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68156398C>T , CM000674.2:g.68156398C>T GRCh38
NC_000012.11:g.68550178C>T , CM000674.1:g.68550178C>T GRCh37
NC_000012.10:g.66836445C>T NCBI36
NG_015840.1:g.8344G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229135.4:c.367-911G>A MANE Select ENSP00000229135.3:n.367-911G>A
ENST00000229135.3:c.367-911G>A ENSP00000229135.3:n.367-911G>A
NM_000619.2:c.367-911G>A NP_000610.2:n.367-911G>A
NM_000619.3:c.367-911G>A MANE Select NP_000610.2:n.367-911G>A
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